ChemicalBook--->CAS DataBase List--->67455-41-8

67455-41-8

67455-41-8 Structure

67455-41-8 Structure
IdentificationBack Directory
[Name]

4-PIPERAZIN-1-YL-PHENYLAMINE
[CAS]

67455-41-8
[Synonyms]

4-PIPERAZINOANILINE
TIMTEC-BB SBB010619
4-PIPERAZIN-1-YLANILINE
4-(4-AMinophenyl)piperazine
4-PIPERAZIN-1-YL-PHENYLAMINE
1-(4-AMINO-PHENYL)-PIPERAZINE
4-(1-Piperazinyl)aniline, 97%
BenzenaMine, 4-(1-piperazinyl)-
1-(4-AMinophenyl)piperazine 97%
Benzenamine, 4-(1-piperazinyl)- (9CI)
4-PIPERAZIN-1-YL-PHENYLAMINE ISO 9001:2015 REACH
[Molecular Formula]

C10H15N3
[MDL Number]

MFCD01365906
[MOL File]

67455-41-8.mol
[Molecular Weight]

177.25
Chemical PropertiesBack Directory
[Melting point ]

119-123 °C(lit.)
[Boiling point ]

380.2±27.0 °C(Predicted)
[density ]

1.107±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C, protect from light
[form ]

Powder
[pka]

9.12±0.10(Predicted)
[color ]

White to purple
[InChI]

1S/C10H15N3/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13/h1-4,12H,5-8,11H2
[InChIKey]

VAVOYRCCWLRTMS-UHFFFAOYSA-N
[SMILES]

Nc1ccc(cc1)N2CCNCC2
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[WGK Germany ]

2
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

4-Piperazinoaniline(CAS#67455-41-8)is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field.
[Synthesis]

1-(4-Nitrophenyl)piperazine

6269-89-2

4-PIPERAZIN-1-YL-PHENYLAMINE

67455-41-8

General procedure for the synthesis of 1-(4-aminophenyl)piperazine from 1-(4-nitrophenyl)piperazine: 1-(4-nitrophenyl)piperazine (414 mg, 2 mmol) was dissolved in a mixed solvent of ethanol (15 mL) and tetrahydrofuran (15 mL), and 10% palladium/carbon catalyst (50 mg) was added. The reaction was stirred for 3 h at room temperature under hydrogen atmosphere. The progress of the reaction was monitored by thin layer chromatography (TLC) during the reaction. Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad to remove the catalyst. The filtrate was concentrated under reduced pressure to afford the target product 1-(4-aminophenyl)piperazine (319 mg, 90.0% yield).

[References]

[1] Synthetic Communications, 2012, vol. 42, # 2, p. 213 - 222
[2] RSC Advances, 2015, vol. 5, # 113, p. 93433 - 93437
[3] Green Chemistry, 2017, vol. 19, # 14, p. 3400 - 3407
[4] Tetrahedron Letters, 1999, vol. 40, # 31, p. 5655 - 5659
[5] Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry, 2011, vol. 41, # 1, p. 114 - 119
Spectrum DetailBack Directory
[Spectrum Detail]

4-PIPERAZIN-1-YL-PHENYLAMINE(67455-41-8)1HNMR
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